VITUS Post-Market Registry
NCT: NCT06832631 · ACTIVE_NOT_RECRUITING
Brief Summary
To collect post marketing surveillance data on consecutive patients with peripheral arterial occlusive disease (PAOD) intended to be or treated by the VITUS peripheral drug-coated dilatation catheter when used according to the Instructions for Use and treating physician decision. Data will be collected in order to assess the long-term safety and performance of the VITUS peripheral drug-coated dilatation catheter in routine clinical practice.
Frequently Asked Questions
What is VITUS Post-Market Registry?
VITUS Post-Market Registry is a clinical trial registered under NCT06832631. Current status: ACTIVE_NOT_RECRUITING.
What is the status of NCT06832631?
The current status of NCT06832631 (VITUS Post-Market Registry) is: ACTIVE_NOT_RECRUITING.
When did VITUS Post-Market Registry start?
VITUS Post-Market Registry started on 2025-05-22.
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Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.